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Scientific Reports
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September 28, 2021
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies
Ben Pode-Shakked, Ortal Barel, Amihood Singer, et al.
American Journal of Human Genetics
|
July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
Dmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
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Search research articles
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Showing results (51-60 of 52) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 52 results.
Scientific Reports
|
September 28, 2021
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies
Ben Pode-Shakked, Ortal Barel, Amihood Singer, et al.
American Journal of Human Genetics
|
July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
Dmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
Page
of 6